Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K9/00—Medicinal preparations characterised by special physical form
  • A61K9/10—Dispersions; Emulsions
  • A61K9/127—Liposomes
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K38/00—Medicinal preparations containing peptides
  • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
  • A61K38/43—Enzymes; Proenzymes; Derivatives thereof
  • A61K38/44—Oxidoreductases (1)
  • A61K38/446—Superoxide dismutase (1.15)
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system

Definitions

• This invention relates to the use of a polypeptide in the preparation of a composition for the treatment of pancreatitis.
• the pancreas comprises exocrine gland tissue, which is 90% of the organ, and endocrine tissue consisting of Langerhans islets.
• Enzymes of pancreatic origin are known, for example protease such as trypsin, chymotrypsin, elastase or leucine aminopeptidase, ⁇ -amylase which hydrolyses ⁇ -1,4-glycoside bonds (hereinafter referred to as amylase), lipase which hydrolyses neutral fat to monoglyceride and fatty acid, cholesterol esterase and phospholipase.
• Insulin is secreted from B-cells in the Langerhans islets and pancreatic glucose is secreted from pancreatic A cells.
• pancreas also secretes various peptide hormones and is controlled by other peptide hormones.
• Pancreatitis is classified in 4 types according to Marseilles' classification, namely acute pancreatitis and chronic pancreatitis each of which is separated into two types, i.e. acute pancreatitis, recurrent acute pancreatitis, chronic pancreatitis and chronic recurrent pancreatitis.
• pancreatitis The main causes of pancreatitis are cholelithiasis and continued over-drinking of alcohol.
• Other types of pancreatitis are, for example, postoperative pancreatitis, parotid gland pancreatitis, parathyroid pancreatitis or drug induced pancreatitis.
• Steroid, chlorothiazid or tetracycline administered induced pancreatitis is also known.
• Clinical diagnosis of pancreatitis is carried out by assaying for increased serum and urinary lipase or amylase activity.
• the polypeptide having superoxide dismutase (hereinafter designated as SOD) activity is useful to scavenge superoxide anion radicals, which are detrimental to cells and tissues. It has been used in the treatment of rheumatic arthritis [Current Therapeutic Res., 20 : 62 - 69 (1976)] and as an anti-inflammatory agent for the skin [PCT. No. 62-501072].
• the present invention provides the use of a polypeptide having superoxide dismutase activity in the preparation of a medicament which comprises liposomes, said liposomes comprising said polypeptide, for the treatment of pancreatitis.
• the present invention also provides the use of a composition which comprises liposomes, said liposomes comprising a polypeptide having superoxide dismutase activity, in the preparation of a medicament for the treatment of pancreatitis.
• the type of polypeptide having SOD activity is not limited. It can be any polypeptide having SOD activity.
• an extracted and purified polypeptide of natural origin a polypeptide prepared by chemical synthesis or genetic engineering means, or a mutein [Glossary of Genetics and Cytogenetics, 4th Ed., p.381 (1976)] which is a partially modified peptide with SOD activity provided by chemical synthesis or genetic engineering, is preferably used.
• polypeptides having SOD activity are polypeptides containing copper and zinc (Cu, Zn-SOD; a dimer, M.W. approx.
• Preferable examples are natural protein delived from bovine liver [ Orgotein, nonproprietary name, the United States Adopted Name Council ; J.A.M.A., 208(8 ): May 26, 1969 ] and polypeptide from human origin [Biochemistry, 19 : 2310-­2316 (1980) and FEBS Letters, 120 : 53 - 55 (1980)] .
• a polypeptide having SOD activity for example a dimer CU, Zn-SOD of human origin polypeptide having SOD activity which is constituted at least 153 amino acids, can be obtained by the following procedures.
• RNA is isolated from human liver tissue, and further poly(A) + RNA is isolated, then c-DNA is synthes­ized therefrom by an ordinal method in genetic engineering thecnique.
• the c-DNA is inserted in a plasmid to prepare an expression vector, which is then transformed into a microorganism such as E. coli and yeast. Then these microorganisms are cultured to produce a dimer polypeptide having SOD activity.
• These genetic engineering thechniques are disclosed in Japanese Patent Unexamined Publication No. 60-137286, ibid. No. 61-111690, ibid. No. 61-139390, ibid. No. 62-115277 and ibid. No. 62-130689.
• a polypeptide having human SOD activity can also be a mutein polypeptide, in which one or more specific part thereof is modified with maintaining SOD activity.
• the expression vector obtained hereinbefore is subjected to a process of site-specific recombination. Namely a closed circular plasmid vector containing DNA corresponding to a polypeptide having natural human type SOD activity therein, is treated with a restriction enzyme Bam HI in the presence of ethidium bromide under dark condition to prepare open circular DNA, which is treated with exonuclease II.
• cysteine at position-6 and/or at position-111 is converted into another amino acid, especially cystein at position-111 is converted to serine, tyrosine, alanine, phenylalanine, tryptophane, arginine, glycine, proline, threonine, histidine, asparagine, aspartic acid, leucine, valine, glutamine, glutamic acid, lysine or methionine, and N-terminal is hydrogen or acetylated group.
• this type mutein polypeptide is a polypeptide having SOD activity in which cysteine at position -6 is cystein per se or is converted to a neutral amino acid such as serine, alanine or threonine, furthermore cysteine at position-111 is converted to a neutral amino acid such as serine, alanine or threonine.
• polypeptides of natural origin and mutein polypeptide having SOD activity are, if required directly or indirectly bound or conjugated with polyalkylene glycol such as molecular weight 400 ⁇ 10,000 polyethylene glycol or polypropylene glycol or ethyleneoxide-propyleneoxide copolymer, at a ratio of 0.5 ⁇ 50 molecule in one molecule of polypeptide to prepare polyethylene derivative of polypeptide.
• polyalkylene glycol such as molecular weight 400 ⁇ 10,000 polyethylene glycol or polypropylene glycol or ethyleneoxide-propyleneoxide copolymer, at a ratio of 0.5 ⁇ 50 molecule in one molecule of polypeptide to prepare polyethylene derivative of polypeptide.
• albumin, styrenemaleic acid or acyl derivative thereof can preferably be prepared.
• polypeptides can also be prepared as a non-­toxic soluble salt thereof.
• a liposome which is preferably applied in the present invention, is defined as a small vesicle consisting of lipid bilayer containing water phase in an inner crust.
• a liposomal preparation of the present invention which contains polypeptide having SOD activity can be produced by known method, for example, disclosed in Biochim. Biophys. Acta, 135 : 624 - 638 (1967), ibid., 443 : 629 - 643 (1976), ibid., 601 559(1980), ibid., 542 137(1978), ibid ., 649 : 129(1981), ibid., 394 483(1975), ibid., 646 1(1 981), ibid., 728 : 339(1983), ibid., 770 : 109(1984), ibid., 817 :193(1985), U.S.
• small-unilamellar vehicle SUV
• large-unilamellar vehicle LUV
• oligolamellar vehicle REV
• multilamellar vehicle MLV
• stable plurilamellar vehicle SPLV
• compositions of liposome itself consists of substantially phospholipid, stabilizing agent and electric charging agent.
• natural or synthetic phospholipid preferably natural phosphatidylcholine such as egg-lecithin and soy bean lecithin or their hydrogenation product, saturated synthetic lecithin such as dimyristoyl­phosphatidylcholine, dipalmitoyl phosphatidylcholine and distearoyl phosphatidylcholine, or unsaturated synthetic lecithin such as dioleoyl phosphatidylcholine and dilinoleoyl phosphatidylcholine, or mixture thereof, or other phosphol­ipid such as sphingomyelin, phosphatidylethanolamine, phosphatidylglycerol, phosphatidylserine and ceramide phosphorylethanolamine, lipid of stabilizing agent such as cholesterol, cationic electric charging agent for liposome such as cetylamine and stearyl
• a prepared lipid composition hereinabove is dissolved in a single or mixed solvent, for example volatile soluble medium such as diethyl ether, chloroform, methylene chloride, ethylacetate, petroleum ether or methanol.
• volatile soluble medium such as diethyl ether, chloroform, methylene chloride, ethylacetate, petroleum ether or methanol.
• the above solution of lipid composition is poured into a round flask and the solvent is removed such as by means of rotary evaporator in order to form thin layer of lipid composition in an inner side of flask. If necessary the operation of adding solvent and removing off is repeated and finally medium should be removed completely in vacuo.
• a solution of polypeptide (0.01 - 100 mg/ml) having SOD activity dissolved in distilled water or buffer solution for injection is added to the lipid composition in the flask at a ratio of 5 - 200 weight parts of the solution to one weight part of lipid composition.
• Amount of polypeptide can be 0.01 - 0.5 weight part in one weight part of lipid composition.
• the mixture is, if required, warmed at 35 - 60 °C in a water-bath, stirred and suspended to obtain liposome solution. Further the suspension is treated with ultrasonication at 10 KC for 1 - 30 min. to prepare liposome of uniform size.
• liposome containing polypeptide having SOD activity mainly consisting of MLV of 50 - 550 nm in diameter can be prepared.
• the thus prepared liposome can be isolated by the centrifugation at 10,000 - 20,000 G for 15 - 60 minutes. Liposome can also be treated by ultracentrifugation for concentration or membrane filtration for sterilization.
• composition for injection can be prepared by suspending the liposome in a liquid for injection to produce suspension, or by adding stabilizing agent for lyophilization such as glucose, sucrose, mannitrol or sorbitol at a concentration of 0.5 ⁇ 10 % to the liposome solution and lyophilizing to produce suspension for intramuscular, subcutaneous or intravenous injection before using.
• stabilizing agent for lyophilization such as glucose, sucrose, mannitrol or sorbitol
• a concentration of polypeptide having SOD activity is controlled to be 0.01 - 100 mg/ml in a liposome preparation for once to fifth times administration in a day with 0.1 - 2 ml in one injection.
• To the liposome preparation can optionally be added an osmotic pressure regulating agent, antiseptics or pH controlling agent.
• Suppositories of the liposome preparation can be also be prepared by mixing a liposome with one or more suppository oleaginous bases, for examples fat and oil, such as olive oil, peanut oil, sesam oil, soybean oil, rapessed oil, camellia oil, cacao butter, lard, lanolin and beef tallow, hydrogenation or acetylation thereof, and emulsified fat and oil with surface active agent, or further adding one or more aqueous base such as glycerogelatin and propyleneglycol therein to prepare 1 ⁇ 2 g per unit of suppository formulation.
• fat and oil such as olive oil, peanut oil, sesam oil, soybean oil, rapessed oil, camellia oil, cacao butter, lard, lanolin and beef tallow
• aqueous base such as glycerogelatin and propyleneglycol
• granules, capsules or syrup formulation can also be prepared by adding ingredients such as fillers, lubricants, sweeteners, color or aroma.
• the thus prepared liposomes containing polypeptide having SOD activity are, as illustrated in the following examples, useful for therapeutic drug composition for pancreatitis which can reduce serum level of lipase and amylase activity on the drug induced pancreatitis cell injury.
• Chloroform solution containing L- ⁇ -dipalmitoyl phosphatidylcholine (hereinafter designates as L- ⁇ -DPPC) 7mM, colesterol 1mM and stearylamine 2mM was prepared.
• Solvent was removed off in vacuo from the above chloroform solution (250 m l, in total containing 3 kinds of lipids hereinabove 2.5 mM), and for further removal of solvent, the mixture was treated in vacuo by oil rotary vacuum pump at approximately few mm Hg for 3 hours to prepare lipid thin layer membrane.
• a phosphate buffer solution (4mM, pH 7.2, 100ml) of polypeptide having human type Cu, Zn-SOD activity (hereinafter designates as SOD-1, 100mg, specific activity 3200 u/mg), wherein cystein at position-111 is site-specifi­cally replaced by serine, which was obtained by culturing E. Coli DH1 carrying plasmid pSOD14 prepared according to a method disclosed in Japanese Patent Unexamined Publication No. 62-130684, was added therein and heated at 40 °C for 6 minutes to disperse lipid, then treated by ultrasonication.
• the prepared liposome containing SOD-1(hereinafter designates as L-SOD-1) has the following properties.
• total activity of SOD was measured by adding 1 % triton X-100 to a sample and incubating at 37°C for 30 minutes.
• SOD-1 was replaced by Cu, Zn-SOD extracted from human erthrocyte (hereinafter designates as SOD-2) [Development in Biochemistry, Biological and Clinical Aspects of Superoxide and Superoxide Dismutase 11B : 348 (1980)] to obtain liposome containing SOD-2 (hereinafter designates as L-SOD-2).
• mice Female Wister rats were divided into 5 groups each of which consists of 5 - 7 rats.
• 4-HAQO dissolved in distilled water for injection was administered intravenously at 20 mg/kg body weight.
• 4-HAQO dissolved in distilled water for injection was administered intravenously at 20 mg/kg body weight, and simultaneo­usly L-SOD-1 suspended in distilled water for injection was administered intraper­itoneally at 16 mg as weight of SOD-1/kg body weight, then after 12 hours same amount of L-SOD-1 (16 mg equivalent to SOD-1) was again administered intraperi­toneally.
• pancreatitis cell damage was assessed by assaying the activities of lipase (Autopack Lip, Tradename Boehringer Mannheim Co.) (Ziegenherm, J. et al., Clin. Chem., 25 : 1067(1979), and Verduin, C.A., et al., Clin. Chim. Acta, 46 : 11(1973) ], and amylase [Clinimate AMY-C, Tradename, Daiichi Kagaku Co.) [Okawa, J. "Clinical Test Technique", vol. 12, p.225(1984), and Kanai, I, Ed. “Clinical Laboratory Tests Commentary", 29th Ed. p.772 (1983)]
• Table 1 Group I II III IV V No. of animals at start 5 7 7 7 6 at biopsy 5 7 7 7 6 lipase 23 1) 147 66 * 56 * 131 (1OU/lit.) ⁇ 10 ⁇ 56 ⁇ 20 ⁇ 18 ⁇ 61 Amylase 31 212 178 175 250 (100 s.u.) ⁇ 4 ⁇ 44 ⁇ 45 ⁇ 42 ⁇ 34 1) Mean ⁇ SD *) significant difference from II Group and V Group at P ⁇ 0.05

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• 1988
  • 1988-03-28 JP JP63073942A patent/JPH01246225A/ja active Pending
• 1989
  • 1989-03-23 DE DE8989302914T patent/DE68906700T2/de not_active Expired - Fee Related
  • 1989-03-23 EP EP89302914A patent/EP0335597B1/fr not_active Expired - Lifetime

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